Evidence map›Paper›PMID 41171737›Full record

ArticlePloS one2025

Structure and function of Full-length Tau.

Laura Vallés-Saiz, Indalo Domene-Serrano, Angel J Picher, Mar Pérez, Vega García-Escudero, Félix Hernández, Jesús Avila

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors.

Laura Vallés-SaizCentro de Biología Molecular Severo Ochoa, CSIC-UAM), Madrid, Spain.
Indalo Domene-SerranoCentro de Biología Molecular Severo Ochoa, CSIC-UAM), Madrid, Spain.ORCID https://orcid.org/0009-0005-1244-1422
Angel J Picher4basebio S.L.U., Parque Científico de Madrid, Cantoblanco, Madrid, Spain.
Mar PérezAnatomy, Histology and Neuroscience Department, School of Medicine, Universidad Autónoma de Madrid (UAM), Madrid, Spain.
Vega García-EscuderoCentro de Biología Molecular Severo Ochoa, CSIC-UAM), Madrid, Spain.ORCID https://orcid.org/0000-0003-1762-0882
Félix HernándezCentro de Biología Molecular Severo Ochoa, CSIC-UAM), Madrid, Spain.ORCID https://orcid.org/0000-0001-8753-8249
Jesús AvilaCentro de Biología Molecular Severo Ochoa, CSIC-UAM), Madrid, Spain.ORCID https://orcid.org/0000-0002-6288-0571

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tau protein, encoded by the MAPT gene, is a microtubule-associated protein involved in the regulation of microtubule stability in neurons, contributing to cell shape maintenance and intracellular transport, among other functions. Tau is not found as a unique isoform; instead, different Tau isoforms of varying sizes are present in the brain, but a Full-length Tau isoform (Full Tau) containing all 16 exons has never been previously identified. This study has explored the structure and function of the Full Tau isoform, which includes all exons of the MAPT gene. To achieve this, we expressed the Full Tau isoform in bacteria, alongside the Tau 4R2N isoform as a control, and tested its microtubule-binding capacity, self-aggregation propensity, and effects on cultured cells regarding cell proliferation and cell death. Our results indicated several differences between the Full Tau and Tau 4R2N isoforms, suggesting distinct roles in cellular dynamics. To explain these differences, we suggest the role of exon 8, which is present in the Full Tau isoform but absent in Tau 4R2N.

Indexed as

tau ProteinsAnimalsCell ProliferationExonsHumansMicrotubulesProtein IsoformsMAPT protein, humanProtein Isoformstau Proteins

Identifiers

PMID41171737
PMCPMC12578172

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.